ATORVASTATIN CALCIUM
- Product NDC
- 63629-4865
- 11-digit product format
- 636294865
- Labeler code
- 63629
- Product ID
- 63629-4865_67497cb8-9c45-4e6f-9f83-7702b9ec4189
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ATORVASTATIN CALCIUM
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA090548
- Marketing category
- ANDA
- Marketing start
- 2012-05-29
- Marketing end
- 0000-00-00
- Substance
- ATORVASTATIN CALCIUM PROPYLENE GLYCOL SOLVATE
- Active strength
- 40 mg/1
- Pharmacologic classes
- HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-4865-1 | 63629486501 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-4865-1) | 2012-12-21 | 0000-00-00 | No | No | Current |
| 63629-4865-2 | 63629486502 | 100 TABLET, FILM COATED in 1 BOTTLE (63629-4865-2) | 2013-08-06 | 0000-00-00 | No | No | Current |
| 63629-4865-3 | 63629486503 | 90 TABLET, FILM COATED in 1 BOTTLE (63629-4865-3) | 2013-05-28 | 0000-00-00 | No | No | Current |
| 63629-4865-4 | 63629486504 | 60 TABLET, FILM COATED in 1 BOTTLE (63629-4865-4) | 2022-03-08 | 0000-00-00 | No | No | Current |
| 63629-4865-5 | 63629486505 | 180 TABLET, FILM COATED in 1 BOTTLE (63629-4865-5) | 2022-03-08 | 0000-00-00 | No | No | Current |
| 63629-4865-6 | 63629486506 | 10 TABLET, FILM COATED in 1 BOTTLE (63629-4865-6) | 2022-03-08 | 0000-00-00 | No | No | Current |